GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **4476 - 4500** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
26531	olfactory receptor family 11 subfamily A member 1	OR11A1
26530	olfactory receptor family 12 subfamily D member 1 (gene/pseudogene)	OR12D1
26529	olfactory receptor family 12 subfamily D member 2	OR12D2
26528	DAZ associated protein 1	DAZAP1
26524	large tumor suppressor kinase 2	LATS2
26523	argonaute RISC component 1	AGO1
26519	translocase of inner mitochondrial membrane 10	TIMM10
26512	integrator complex subunit 6	INTS6
26509	myoferlin	MYOF
26505	cyclin and CBS domain divalent metal cation transport mediator 3	CNNM3
26504	cyclin and CBS domain divalent metal cation transport mediator 4	CNNM4
26503	solute carrier family 17 member 5	SLC17A5 AST ISSD NSD SD SIALIN SLD Salla disease acidic sugar transporter infantile sialic acid storage disorder	Alzheimer's disease Balo concentric sclerosis Crimean-Congo hemorrhagic fever Gilbert syndrome HELLP syndrome IgA glomerulonephritis Japanese encephalitis Lassa fever Parkinson's disease Plasmodium falciparum malaria Reye syndrome Stevens-Johnson syndrome Wilson disease abdominal obesity-metabolic syndrome 1 acrodermatitis acute pancreatitis adrenoleukodystrophy agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma alternating exotropia amelogenesis imperfecta type 1E amnestic disorder amyotrophic lateral sclerosis type 1 anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hepatitis autoimmune polyendocrine syndrome bilirubin metabolic disorder cancer cardiovascular system disease cataract 2 multiple types cataract 30 cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chromosome 17p13.1 deletion syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common cold communicating hydrocephalus congenital nystagmus congenital ptosis congestive heart failure coronary artery disease dementia dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism disseminated intravascular coagulation dissociated nystagmus dysthymic disorder embryoma epilepsy essential hypertension essential thrombocythemia exotropia familial hyperlipidemia familial nephrotic syndrome fascioliasis fibromyalgia gallbladder disease gingival hypertrophy gingival overgrowth glomerulonephritis glucose intolerance glycogen storage disease II head and neck squamous cell carcinoma heart disease hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hyperglycemia hypertension hypohidrotic ectodermal dysplasia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome intellectual disability intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy leukopenia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung cancer lung non-small cell carcinoma lymphopenia lysosomal storage disease macrocytic anemia major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma microphthalmia monocular exotropia myelodysplastic syndrome myocarditis myositis narcolepsy nasopharyngitis nephritis nephrosis nephrotic syndrome neurodegenerative disease neurotic disorder neutropenia obesity obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteoarthritis osteomalacia pancreatitis pancytopenia parapsoriasis pathologic nystagmus pneumonia portal vein thrombosis pre-eclampsia prediabetes syndrome primary polycythemia primary sclerosing cholangitis psoriasis ptosis purpura fulminans pustulosis of palm and sole pyoureter retrograde amnesia rheumatoid arthritis rickets sclerosing cholangitis senile degeneration of brain severe congenital neutropenia sialuria sickle cell anemia skin melanoma spontaneous ocular nystagmus steatotic liver disease subcortical band heterotopia thrombocytopenia tuberculosis type 2 diabetes mellitus uremia viral infectious disease visceral leishmaniasis visual epilepsy yellow fever
26496	olfactory receptor family 10 subfamily A member 3	OR10A3
26494	olfactory receptor family 8 subfamily G member 1	OR8G1
26493	olfactory receptor family 8 subfamily B member 8	OR8B8
26476	olfactory receptor family 10 subfamily J member 1	OR10J1
26470	seizure related 6 homolog like 2	SEZ6L2
26354	G protein nucleolar 3	GNL3
26353	heat shock protein family B (small) member 8	HSPB8
26341	olfactory receptor family 5 subfamily H member 1	OR5H1
26339	olfactory receptor family 5 subfamily K member 1	OR5K1
26338	olfactory receptor family 5 subfamily L member 2	OR5L2
26333	olfactory receptor family 7 subfamily A member 17	OR7A17
26330	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	GAPDHS GAPD2 GAPDH-2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Pick's disease Reye syndrome cancer cerebral degeneration diabetes mellitus diabetic ketoacidosis embryoma melanoma skin melanoma
26301	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)	GBGT1 A3GALNT FS Forssman blood group Forssman glycolipid synthetase (FS) Forssman synthetase MGC44848 UDP-GalNAc	cancer celiac disease embryoma ovarian cancer ovarian carcinoma thrombophilia

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